rs2394985
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2394985(C;T) |
Make rs2394985(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355780 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs2394985 |
dbSNP (classic) | rs2394985 |
ClinGen | rs2394985 |
ebi | rs2394985 |
HLI | rs2394985 |
Exac | rs2394985 |
Gnomad | rs2394985 |
Varsome | rs2394985 |
LitVar | rs2394985 |
Map | rs2394985 |
PheGenI | rs2394985 |
Biobank | rs2394985 |
1000 genomes | rs2394985 |
hgdp | rs2394985 |
ensembl | rs2394985 |
geneview | rs2394985 |
scholar | rs2394985 |
rs2394985 | |
pharmgkb | rs2394985 |
gwascentral | rs2394985 |
openSNP | rs2394985 |
23andMe | rs2394985 |
SNPshot | rs2394985 |
SNPdbe | rs2394985 |
MSV3d | rs2394985 |
GWAS Ctlg | rs2394985 |
GMAF | 0.0124 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2394985(T;T) |
Alt | rs2394985(T;T) |
Reference | Rs2394985(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31323557C>T |
CLNSRC | |
CLNACC |